Draw the product formed when diene and dienophile react in a Diels–Alder reaction.

Explanation:

Diels-Alder reactions are cyclo-additional reactions between conjugated dienes and a dienophile (a substituted alkene compound for example acrylic acid) to produce a ring structure of cyclohexene compounds.

From the image attached below, we will see the reaction between 2,3-dimethylbuta-1,3-diene which is a conjugated diene with acrylic acid to produce a Diel-Alder adduct as the product.  From the reaction, a single new π-bond and two σ-bonds are produced.

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explanation:

answer: - 3.) the oxidation state of nitrogen in no changes from +2 to 0, and the oxidation state of carbon in co changes from +2 to +4 as the reaction proceeds.

solution: - as per the rules, oxidation number of oxygen in its compounds is -2. the sum of oxidation numbers of all the elements of a molecule or compound is zero.

also, the oxidation number in elemental form is zero.

in no, the oxidation number of o is -2 so the oxidation number of n is +2 so that the sum is zero.

similarly, the oxidation number of c in co is +2 and o is -2.

on product side the oxidation number of n is 0 as it is in the elemental form() .

oxidation number of c in carbon dioxide is +4 as there are two oxygen in it and we know that each oxygen is -2.

so, oxidation number of n is changing from +2 to 0 and the oxidation number of c is changing from +2 to +4.

since nitrogen is reduced and hence no is acting as an oxidizing agent. carbon is oxidized and so co is acting as a reducing agent.

so, the right choice is number 3.)the oxidation state of nitrogen in no changes from +2 to 0, and the oxidation state of carbon in co changes from +2 to +4 as the reaction proceeds.